Are you familiar with the jungle of regulations? Have you really thought about everything?
Take advantage of our expertise even during the development of your ATMP so that there are no time-consuming detours on the way to production and approval!
You are busy with the development of an exciting ATMP and planning of production and approval are the next steps to think about? Therefore you want to make sure that you follow the AMG and the ATMP-GMP guidelines and that your processes, premises and equipment is in compliance with the regulatory requirements? Are you planning or looking for a suitable production site to manufacture your ATMP investigational medicinal production?
Valicare’s scientists and GMP experts support you during development. They validate your process and transfer it into the GMP environment right through to production, approval or hospital exemption of your ATMP. With a risk-based approach, state-of-the-art science and technology and always in compliance with the required regulation, our experts get your product ready for market!
GMP and especially ATMP GMP seminars, but also on-site training to ensure GMP-compliant behavior during whole production processes of ATMP are part of our services, too.
If you work with us, you decide for:
(according to your tariff for calls to the German landline)
or fill in our contact form:
Our GMP consultants will reply to you as soon as possible without any obligation.
The items marked with * are mandatory.
